Project Description
Dr. Steven Forman joined Los Alamitos Cardiovascular in 1999 and has been its managing partner since 2005. In addition to his roles at Los Alamitos Cardiovascular, Dr. Forman is director of Performance Vein Institute of Los Alamitos—a practice focused on the diagnosis and treatment of vein disease of the lower extremities. Dr. Forman is board certified in Interventional Cardiology, Cardiovascular Disease and Venous and Lymphatic Medicine. In December 2015, he completed a two-year term as chief of staff at Los Alamitos Medical Center (LAMC), and since 2014, Dr. Forman has been the director of LAMC’s Cardiac Catheterization Lab. In 2018, Dr. Forman became chairperson of LAMC’s Board of Governors.
Dr. Steven T. Forman’s Curriculum Vitae
Specialties:
Cardiology, Interventional Cardiology, Endovascular Diseases, Venous and Lymphatic Medicine
Board Certifications:
- Certified in Venous and Lymphatic Medicine
American Board of Venous and Lymphatic Medicine (ABVLM) 2012 - Certified in Interventional Cardiology
American Board of Internal Medicine
1999 (Recertification 2009) - Certified in Cardiovascular Disease
American Board of Internal Medicine
1997 (Recertification 2017) - Expert Reviewer
The Medical Board of California
August 2014-Present
Additional Certifications:
- GCP Certified July 2010
CITI Collaborative Institutional Training Initiative
Current Hospital Appointments:
- Los Alamitos Medical Center
3751 Katella Avenue
Los Alamitos, California 90720 - MemorialCare Health System
Long Beach Memorial Medical Center
2801 Atlantic Avenue
Long Beach, California 90801 - Lakewood Regional Medical Center
3700 South Street
Lakewood, California 90712
Committees:
Los Alamitos Medical Center
- Chairman, Board of Governors
January 2018 – December 2019 - Director of Cardiac Catheterization Lab
Effective March 2014 - Chief of Staff
January 2013 – December 2014 - Chairman of Elective PCI Pilot Program
June 2010 – 2014 - Vice Chief of Staff, Medical Executive Committee
January 2012 – December 2013 - Secretary/Treasurer, Medical Executive Committee
January 2010 – December 2011 - Chief of Medicine
January 2007 – December 2010 - Chairman of Allied Health Committee
January 2006 – December 2006 - Member, Medical Executive Committee
January 2006 – Present - Member, Myocardial Infarction Quality Assurance Committee
January 2001 – Present - Member, Cardiovascular Quality Assurance Committee
January 2000 – Present
State of California
- Member, AOC (Advisory Oversight Committee) for the Elective PCI (Percutaneous Coronary Interventions) Pilot Program for the State of California
June 2010 – 2014
Professional Societies:
- American College of Phlebology (RVT)
Member - American College of Cardiology (FACC)
Fellow - American College of Physicians (FACP)
Member - Society for Cardiovascular Angiography and Intervention
Member
Academic Appointments:
- Volunteer Faculty
Department of Medicine/Division of Cardiology
University of California , Irvine (UCI)
November 2011 – Present - Instructor in Medicine
Department of Medicine
The New York Hospital /Cornell University Medical Center
June 1996 – June 1998
Work History:
- Los Alamitos Cardiovascular
Los Alamitos, California
1999 – Present - Cardiology Associates of North Jersey
1030 Clifton Avenue
Clifton, New Jersey 07013
July 1998 – August 1999 - Urgent Care Physician
Memorial Sloan Kettering Cancer Center
New York, New York
July 1994 – June 1996
Previous Hospital Appointments:
- General Hospital of Passaic
350 Boulevard
Passaic, New Jersey 07055
July 1998 – August 1999 - Saint Mary’s Hospital
211 Pennington Avenue
Passaic, New Jersey 07055
July 1998 – August 1999 - Saint Joseph’s Hospital and Medical Center
703 Main Street
Passaic, New Jersey 07055
July 1998 – August 1999 - Chilton Memorial Hospital
97 West Parkway
Pomptom Plains, New Jersey 07444
July 1998 – August 1999 - Passaic Beth Israel Hospital
70 Parker Avenue
Passaic, New Jersey 07055
July 1998 – August 1999
Publications:
- Shaknovich A, Forman ST, Parikh M, Deutsch E, Bergman G, McCaffery T, Newman GC, Tarazona N and Sanborn T. “Novel distal occluder washout methods for prevention of no-reflow during stenting of saphenous vein grafts.” Catheter Cardiovascular Intervention. 1999 Aug: 47(4): 397 – 403.
- Marshall ES, Raichlen JS, Forman S, Heyrich GP, Keen WD, Weitz HH. “Adenosine radionuclide perfusion imaging in the preoperative evaluation of patients undergoing peripheral vascular surgery.” American Journal of Cardiology. 1995 Oct 15: 76(11): 817 – 821.
Education:
- Interventional Cardiology Fellowship
The New York Hospital – Cornell University Medical Center
The Division of Cardiology
New York, New York
July 1997 – June 1998 - Cardiovascular Diseases Fellowship
The New York Hospital – Cornell University Medical Center
New York, New York
July 1994 – June 1997 - Internal Medicine Internship and Residency
Thomas Jefferson University Hospital
Department of Medicine
Philadelphia, Pennsylvania
July 1991 – June 1994 - Medical Education
Albany Medical College
Albany, New York
MD, May 1991 - Undergraduate Education
The Johns Hopkins University
Baltimore, Maryland
Bachelor of Arts in Natural Science, May 1987
Research Experience:
- AEGIS: A Phase 3, Multicenter, Double-blind, Randomized, Placebo-controlled, Parallel-group Study to Investigate the Efficacy and Safety of CSL112 in Subjects with Acute Coronary Syndrome.
Sub-Investigator | 2019
Sponsor: CSL Behring LLC
NCT03473223: https://clinicaltrials.gov/ct2/show/NCT03473223 - COVET : Comparison of Oral anticoagulants for extended Venous Thromboembolism (COVET). It is a randomized, open label, active comparator to determine whether the direct oral anticoagulant apixaban and rivaroxaban are safer than warfarin (fewer bleeding complications) and still as effective as warfarin (no increase in recurrent blood clots).
Principal Investigator | 2018 – Present
Sponsor : Patient-Centered Outcomes Research Institute (PCORI)
NCT03196349: https://clinicaltrials.gov/ct2/show/NCT03196349 - NODE 301: Multi-Centre, Randomized, Double-Blind, Placebo-Controlled, Efficacy, and Safety Study of Etripamil Nasal Spray for the Termination of Spontaneous Episodes of Paroxysmal Supraventricular Tachycardia.
Sub-Investigator | 2019
Sponsor: Milestone Pharmaceuticals Inc.
NCT03464019: https://clinicaltrials.gov/ct2/show/NCT03464019 - NODE 302: Multi-Centre, Open-Label, Safety Study of Etripamil Nasal Spray in Spontaneous Episodes of Paroxysmal Supraventricular Tachycardia (Extension of NODE-301).
Sub-Investigator | 2019
Sponsor: Milestone Pharmaceuticals Inc.
NCT03635996: https://clinicaltrials.gov/ct2/show/NCT03635996 - PARADISE MI: A multi-center, randomized, double-blind, active-controlled, parallel-group Phase 3 study to evaluate the efficacy and safety of LCZ696 compared to ramipril on morbidity and mortality in high risk patients following an acute myocardial infarction.
Sub-Investigator | 2018 – Present
Sponsor: Novartis
NCT02924727: https://clinicaltrials.gov/ct2/show/NCT02924727 - PEA-VALVE: Phono- and Electrocardiogram Assisted Detection of Valvular Disease. This is data collection of recorded heart sounds + ECGs using Eko Duo and Eko Core devices to further refine and validate algorithms using de-identified diagnosis confirmed by gold-standard echocardiograms.
Principal Investigator | 2018 – Present
Sponsor: Eko Devices - GALACTIC-HF: Double-blind, Randomized, Placebo-controlled, Multicenter Study to Assess the Efficacy and Safety of Omecamtiv Mecarbil on Mortality and Morbidity in Subjects With Chronic Heart Failure With Reduced Ejection Fraction.
Principal Investigator | 2017 – Present
Sponsor: Amgen
NCT02929329 | https://clinicaltrials.gov/ct2/show/NCT02929329 - PROVE-HF: A 52 Week, Open Label Evaluation of the Effects of Sacubitril/Valsartan (LCZ696) Therapy on Biomarkers, Myocardial Remodeling and Patient-reported Outcomes in Heart Failure With Reduced Left Ventricular Ejection Fraction.
Sub-Investigator | 2017 – 2019
Sponsor: Novartis
NCT02887183 | https://clinicaltrials.gov/ct2/show/NCT02887183 - Barostim Therapy for Heart Failure (BeAT-HF): The Barostim Neo – Baroreflex Activation Therapy for Heart Failure is a prospective, randomized trial in subjects with reduced ejection fraction heart failure.
Principal Investigator | 2016 – Present
Sponsor: CVRx, Inc.
NCT02627196 | https://clinicaltrials.gov/show/NCT02627196 - MLHFQ Study: Evaluate and establish content validity of the Minnesota Living with Heart Failure Questionnaire (MLHFQ) in patients with Symptomatic Hypertrophic Cardiomyopathy.
Principal Investigator | 2016 – 2017
Sponsor: Gilead/ICON - THEMIS- A Study Comparing Cardiovascular Effects of Ticagrelor Versus Placebo in Patients With Type 2 Diabetes Mellitus (THEMIS): A Multinational, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Effect of Ticagrelor Twice Daily on the Incidence of Cardiovascular Death, Myocardial Infarction or Stroke in Patients With Type 2 Diabetes Mellitus (THEMIS – Effect of Ticagrelor on Health Outcomes in Diabetes Mellitus Patients Intervention Study).
Sub-Investigator | 2015 – Present
Sponsor: AstraZeneca
NCT01991795 | https://clinicaltrials.gov/show/NCT01991795 - Retrospective Medical Records Review of Participants Interviewed for Study M-12347 (Concept Elicitation Focus Groups and Cognitive Interviews to Develop a New Patient Reported Outcome Instrument in Chronic Heart Failure).
Sub-Investigator | 2015 – 2016
Sponsor: Amgen, Evidera - DECLARE-TIMI 58 Dapagliflozin Effect on CardiovascuLAR Events: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Effect of Dapagliflozin 10 mg Once Daily on the Incidence of Cardiovascular Death, Myocardial Infarction or Ischemic Stroke in Patients with Type 2 Diabetes.
Principal Investigator | 2013 – 2018
Sponsor: AstraZeneca
NCT01730534 | https://clinicaltrials.gov/ct2/show/NCT01730534 - ODYSSEY EFC11570: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Effect of SAR236553/REGN727 on the Occurrence of Cardiovascular Events in Patients Who Have Recently Experienced an Acute Coronary Syndrome
Sub-Investigator | 2013 – 2017
Sponsor: Sanofi
NCT01663402 | https://clinicaltrials.gov/ct2/show/NCT01663402 - SILVER-AMI Risk Stratification in Older Persons with Acute Myocardial Infarction.
Sub-Investigator | 2013 – 2017
Sponsor: Yale University School of Medicine/NIH
NCT01755052 | https://clinicaltrials.gov/ct2/show/NCT01755052 - RivaroxAFL3003: An Open Label Study Exploring two treatment strategies in patients with Atrial Fibrillation who undergo Percutaneous Coronary Intervention.
Principal Investigator | 2013 – 2014
Sponsor: Janssen Scientific Affairs/Johnson & Johnson - Phase III Trial to confirm the Anti-Anginal effect of T-89 in patients with Stable Angina.
Principal Investigator | 2013
Sponsor: Tasly Pharmaceuticals
NCT0169580 | https://clinicaltrials.gov/ct2/show/NCT01659580 - Cardiovascular Inflammation Reduction Trial (CIRT): Event Driven Trial of weekly Low-Dose Methotrexate in prevention of recurrent cardiovascular events among stable post myocardial infarction patients with Type II Diabetes or Metabolic Syndrome.
Principal Investigator | 2013 – 2018
Sponsor: Center for Cardiovascular Disease Prevention Brigham and Women’s Hospital/National Heart Lung and Blood Institute
NCT01594333 | https://clinicaltrials.gov/ct2/show/NCT01594333 - User Comprehension Evaluation of a New Cleaning and Disinfection Procedure for the INRatio® 2PT/INR Monitoring System (ADAPT) BSTE-0159.
Principal Investigator | 2012
Sponsor: Alere San Diego - Mission® PT Coagulation Monitoring System Clinical Study.
Sub-Investigator | 2012
Sponsor: ACON Laboratories, INC. - The “BRIDGE” Trial (1U01HL08675501A1): Bridging Anticoagulation in Patients Who Require Temporary Interruption of Warfarin Therapy for an Elective Invasive Procedure or Surgery.
Principal Investigator | 2012 – 2015
Sponsor: National Institutes of Health (NIH)-National Heart, Lung and Blood Institute (NHLBI)
NCT00786474 | https://clinicaltrials.gov/ct2/show/NCT00786474 - GLORIA-AF 1160.129: Global Registry on Long-Term Oral Anti-thrombotic Treatment in Patients with Atrial Fibrillation Phase II-III.
Principal Investigator | 2012 – Present
Sponsor: Boehringer Ingelheim
NCT01468701 | https://clinicaltrials.gov/ct2/show/NCT01468701 - California State Elective Percutaneous Coronary Intervention Pilot Program
Principal Investigator | 2010 – 2014 - BRADYCARE: Advanced Bradycardia Device Feature Utilization and Clinical Outcomes.
Sub-Investigator | 2010 – 2012
Sponsor: St. Jude Medical Center
NCT01062126 | https://clinicaltrials.gov/ct2/show/NCT01062126 - The PROMISE Trial: PROspective Multicenter Imaging Study for Evaluation of Chest Pain.
Principal Investigator | 2010 – 2014
Sponsor: National Heart, Lung, and Blood Institute (NHLBI)
NCT01174550 | https://clinicaltrials.gov/ct2/show/NCT01174550 - ORBIT-AF I and II: Outcomes Registry for Better Informed Treatment of Atrial Fibrillation.
Principal Investigator | 2010 – 2017
Sponsor: Janssen Scientific Affairs, LLC
Collaborator: Duke Clinical Research
NCT01165710 | https://clinicaltrials.gov/ct2/show/NCT01165710
NCT01701817 | https://clinicaltrials.gov/ct2/show/NCT01701817 - RATE: Registry of Atrial Tachyarrhythmia/Atrial Fibrillation (AT/AF) Episodes in the Cardiac Rhythm Management (CRM) Device Population.
Sub-Investigator | 2008 – 2010
Sponsor: St. Jude Medical Center
NCT00837798 | https://clinicaltrials.gov/ct2/show/NCT00837798 - FREEDOM: A Frequent Optimization Study the Quick Opt ™ Method.
Sub-Investigator | 2008 – 2010
Sponsor: St. Jude Medical Center
NCT00418314 | http://clinicaltrials.gov/ct2/show/NCT00418314 - ENGAGE: Phase III, randomized, double-blind, double-dummy, parallel group, multi-center, multi-national study for evaluation of efficacy and safety of DU-176b versus Warfarin in subjects with Atrial Fibrillation – Effective Anticoagulation with Xa next Generation in Atrial Fibrillation (ENGAGE – AF TIMI – 48).
Principal Investigator | 2009 – 2015
Sponsor: Daiichi Sankyo Pharma Development
NCT00781391 | http://clinicaltrials.gov/ct2/show/NCT00781391 - Phase III, double-blind, randomized, placebo-controlled, multi-center study evaluating the efficacy and safety of Dalcetrapib on lipids, lipoproteins, apolipoproteins and markers of CV Risk in patients hospitalized for an acute coronary syndrome (ACS) when treatment is initiated within 1 week after an ACS (Dal-ACUTE).
Principal Investigator | 2008 – 2012
Sponsor: F.Hoffmann-La Roche Ltd., Hoffmann-La Roche, Inc. , Roche Global Development.
NCT01323153 | https://clinicaltrials.gov/ct2/show/NCT01323153 - Multi-center, randomized, controlled study to investigate the safety and tolerability of Intravenous Ferric Carboxymaltose (FCM) vs. Iron Dextran in treating iron deficiency anemia in subjects who are not dialysis dependent.
Principal Investigator | 2007 – 2009
Sponsor: Luitpold Pharmaceuticals, Inc.
NCT00704028 | https://clinicaltrials.gov/ct2/show/NCT0070402 - Systolic and diastolic myocardial dysfunction during endotoxemia in pigs. Proctor: Roy D Goldfarb, Phd | 1989 – 1991
Department of Physiology, Albany Medical College